TENDERSANT HAND SANITIZER- alcohol gel

Tendersant Hand Sanitizer by

Drug Labeling and Warnings

Tendersant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Geri-Gentle Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses:

To decrease bacteria on the skin.

Recommended for repeated use.

Warnings

Keep away from fire or flame. Flammable.

Avoid contact with broken skin. For external use only.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use:

if irritation or redness develops.

• If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children

If swallowed, get medical help

Directions:

Not recommended for infants

• Wet hands thoroughly with product and allow to dry without wiping
• Children under 6 years of age should be supervised when using this product.

Other information:

Do not store above 110°F,

May discolor some fabrics..

Inactive ingredients:

Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate crosspolymer, Triethanolamine, Fragrance.

Package Labeling:118ml

Package Labeling:500ml

Package Labeling:236ml

INGREDIENTS AND APPEARANCE

TENDERSANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69771-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69771-007-01	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
2	NDC: 69771-007-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
3	NDC: 69771-007-03	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/01/2020

Labeler - Geri-Gentle Corporation (080367686)